Toxic mechanism of eucalyptol and β-cyclocitral on Chlamydomonas reinhardtii by inducing programmed cell death

被引:28
|
作者
Sun, Qing [1 ,2 ]
Zhou, Min [1 ,2 ]
Zuo, Zhaojiang [1 ,2 ]
机构
[1] Zhejiang A&F Univ, State Key Lab Subtrop Silviculture, Hangzhou 311300, Peoples R China
[2] Zhejiang A&F Univ, Sch Forestry & Biotechnol, Hangzhou 311300, Peoples R China
基金
中国国家自然科学基金;
关键词
Chlamydomonas reinhardtii; Cyanobacteria; beta-Cyclocitral; Eucalyptol; Programmed cell death; VOLATILE ORGANIC-COMPOUNDS; OXYGEN SPECIES GENERATION; MICROCYSTIS-AERUGINOSA; OXIDATIVE STRESS; PHOTOSYNTHETIC ABILITIES; ANTIFUNGAL ACTIVITY; COMPOUND EMISSIONS; HYDROGEN-PEROXIDE; PYROGALLIC ACID; ODOR COMPOUNDS;
D O I
10.1016/j.jhazmat.2019.121910
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Eucalyptol and beta-cyclocitral are 2 main compounds in cyanobacterial volatile organic compounds and can poison other algae. To uncover the toxic mechanism of the 2 compounds, the cell growth, photosynthetic abilities, H2O2 production, caspase-like activities, nuclear variation and DNA laddering were investigated in Chlamydomonas reinhardtii treated with eucalyptol and beta-cyclocitral. Eucalyptol at >= 0.1 mM and beta-cyclocitral at >= 0.05 mM showed toxic effects on C. reinhardtii cells, and 1.2 mM eucalyptol and 0.4 mM beta-cyclocitral killed the whole of the cells during 24 h. During the death process, the photosynthetic pigment gradually degraded, and Fv/Fm gradually declined, indicating that the death is not a necrosis due to the gradual disappearance of the physiological process. In the treatments with 1.2 mM eucalyptol and 0.4 mM beta-cyclocitral, H2O2 content burst at 10 min and 30 min, respectively. Caspase-9-like and caspase-3-like were activated, and cell nucleuses concentrated firstly and then broke with prolonging the treatment time. Meanwhile, DNA showed laddering after 1 h, and was gradually cleaved by Ca2+-dependent endonucleases to mainly about 100-250 bp fragments. These hallmarks indicated that eucalyptol and beta-cyclocitral may poison other algal cells by inducing programmed cell death triggered by the increased H2O2.
引用
收藏
页数:9
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